All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00892 FIH1 hypoparathyroidism, familial isolated, type 1 (FIH) 146200 AD;AR - - GCM2, PTH - autosomal dominant
06730 FIH2 Hypoparathyroidism, familial isolated 2 618883 - - - GCM2 - -
06698 HRPT4 Hyperparathyroidism 4 617343 AD - - GCM2 - -
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